Evidence map›Paper›PMID 37864843›Full record

ArticleMedical physics2024

Enhancing cerebral vasculature analysis with pathlength-corrected 2D angiographic parametric imaging: A feasibility study.

Allison Shields, Kyle Williams, Mohammad Mahdi Shiraz Bhurwani, Swetadri Vasan Setlur Nagesh, Venkat Keshav Chivukula, Daniel R Bednarek, Stephen Rudin, Jason Davies, Adnan H Siddiqui, Ciprian N Ionita

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Article in Medical physics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.2field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 6 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Allison ShieldsMedical Physics Program, University at Buffalo, Buffalo, New York, USA.
Kyle WilliamsMedical Physics Program, University at Buffalo, Buffalo, New York, USA.
Mohammad Mahdi Shiraz BhurwaniQAS.AI Inc, Buffalo, New York, USA.
Swetadri Vasan Setlur NageshMedical Physics Program, University at Buffalo, Buffalo, New York, USA.
Venkat Keshav ChivukulaDepartment of Biomedical Engineering, Florida Institute of Technology, Melbourne, Florida, USA.
Daniel R BednarekMedical Physics Program, University at Buffalo, Buffalo, New York, USA.
Stephen RudinMedical Physics Program, University at Buffalo, Buffalo, New York, USA.
Jason DaviesCanon Stroke and Vascular Research Center, University at Buffalo, Buffalo, New York, USA.
Adnan H SiddiquiCanon Stroke and Vascular Research Center, University at Buffalo, Buffalo, New York, USA.
Ciprian N IonitaMedical Physics Program, University at Buffalo, Buffalo, New York, USA.
University at Buffalo, State University of New York · USBuffalo VA Medical Center · USFlorida Institute of Technology · USJacobs Institute · US

Funding

High Speed Angiography at 1000 frames per secondR01EB030092 · NIBIB · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI RUDIN, STEPHEN · 2020 to 2023
$2.6M
NIBIB NIH HHS R01 EB030092NIH HHS 1R01EB030092
6 · The paper itself

Abstract

background2D angiographic parametric imaging (API) quantitatively extracts imaging biomarkers related to contrast flow and is conventionally applied to 2D digitally subtracted angiograms (DSA's). In the interventional suite, API is typically performed using 1-2 projection views and is limited by vessel overlap, foreshortening, and depth-integration of contrast motion. PURPOSE: This work explores the use of a pathlength-correction metric to overcome the limitations of 2D-API: the primary objective was to study the effect of converting 3D contrast flow to projected contrast flow using a simulated angiographic framework created with computational fluid dynamics (CFD) simulations, thereby removing acquisition variability.

methodsThe pathlength-correction framework was applied to in-silico angiograms, generating a reference (i.e., ground-truth) volumetric contrast distribution in four patient-specific intracranial aneurysm geometries. Biplane projections of contrast flow were created from the reference volumetric contrast distributions, assuming a cone-beam geometry. A Parker-weighted reconstruction was performed to obtain a binary representation of the vessel structure in 3D. Standard ray tracing techniques were then used to track the intersection of a ray from the focal spot with each voxel of the reconstructed vessel wall to a pixel in the detector plane. The lengths of each ray through the 3D vessel lumen were then projected along each ray-path to create a pathlength-correction map, where the pixel intensity in the detector plane corresponds to the vessel width along each source-detector ray. By dividing the projection sequences with this correction map, 2D pathlength-corrected in-silico angiograms were obtained. We then performed voxel-wise (3D) API on the ground-truth contrast distribution and compared it to pixel-wise (2D) API, both with and without pathlength correction for each biplane view. The percentage difference (PD) between the resultant API biomarkers in each dataset were calculated within the aneurysm region of interest (ROI).

resultsIntensity-based API parameters, such as the area under the curve (AUC) and peak height (PH), exhibited notable changes in magnitude and spatial distribution following pathlength correction: these now accurately represent conservation of mass of injected contrast media within each arterial geometry and accurately reflect regions of stagnation and recirculation in each aneurysm ROI. Improved agreement was observed between these biomarkers in the pathlength-corrected biplane maps: the maximum PD within the aneurysm ROI is 3.3% with pathlength correction and 47.7% without pathlength correction. As expected, improved agreement with ROI-averaged ground-truth 3D counterparts was observed for all aneurysm geometries, particularly large aneurysms: the maximum PD for both AUC and PH was 5.8%. Temporal parameters (mean transit time, MTT, time-to-peak, TTP, time-to-arrival, TTA) remained unaffected after pathlength correction.

conclusionsThis study indicates that the values of intensity-based API parameters obtained with conventional 2D-API, without pathlength correction, are highly dependent on the projection orientation, and uncorrected API should be avoided for hemodynamic analysis. The proposed metric can standardize 2D API-derived biomarkers independent of projection orientation, potentially improving the diagnostic value of all acquired 2D-DSA's. Integration of a pathlength correction map into the imaging process can allow for improved interpretation of biomarkers in 2D space, which may lead to improved diagnostic accuracy during procedures involving the cerebral vasculature.

Indexed as

AngiographyIntracranial AneurysmArteriesBiomarkersFeasibility StudiesHumansImaging, Three-DimensionalBiomarkerscomputational fluid dynamicshemodynamicsquantitative angiography

Identifiers

PMID37864843
PMCPMC10994741
OpenAlexW4387848605

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.